药品名称HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号019953产品号001
活性成分HEPARIN SODIUM市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格200 UNITS/100ML
治疗等效代码AP参比药物
批准日期1992/07/20申请机构B BRAUN MEDICAL INC
化学类型New formulation or new manufacturer审评分类Standard review drug
与本品相关的专利信息(来自橙皮书Orange Book)
专利号专利过期日是否化合物专利是否产品专利专利用途代码专利下载
历史专利信息
与本品相关的市场独占权保护信息
独占权代码失效日期
历史市场独占权保护信息
与药品注册相关的信息
申请号修订号审批结论公开文档类型文档创建时间获取文档
019953032APLetter2016/05/16下载
019953032APLabel2016/05/17下载
019953030APLetter2013/09/04下载
019953030APLabel2013/09/09下载
019953029APLabel2013/01/11下载
019953029APLetter2013/01/14下载
019953025APLabel2011/12/23下载
019953025APLetter2011/12/29下载
019953021APLetter2009/03/03下载
019953021APLabel2009/03/17下载
019953012APLetter2004/04/20下载
药品注册审批历史信息
申请号修订号审批结论审批日期审批内容
019953032AP2016/05/12Labeling Revision
019953030AP2013/08/30Labeling Revision
019953029AP2013/01/10Labeling Revision
019953025AP2011/12/27Labeling Revision
019953021AP2009/02/26Labeling Revision
019953020AP2014/08/22Manufacturing Change or Addition
019953012AP2004/04/13Labeling Revision
019953011AP2002/07/12Control Supplement
019953009AP2002/02/15Package Change
019953008AP2000/11/22Control Supplement
019953007AP2000/03/01Control Supplement
019953006AP1998/06/05Control Supplement
019953005AP1996/07/30Manufacturing Change or Addition
019953004AP1995/03/09Control Supplement
019953003AP1992/12/22Labeling Revision
019953002AP1992/12/02Manufacturing Change or Addition
019953001AP1993/03/29Package Change
019953000AP1992/07/20Approval